Primary explosives

ABSTRACT

The present invention provides a compound of the formula (Cat) +   z [M ++ (5-nitro-1H-tetrazolato-N2) −   x (H 2 O) y ] where x is 3 or 4, y is 2 or 3, x+y is 6, z is 1 or 2, and M ++  is selected from the group consisting of iron, cobalt, nickel, copper, zinc, chromium, and manganese, and (Cat) +  is selected from the group consisting of ammonium, sodium, potassium, rubidium and cesium. A method of preparing the compound of that formula is also disclosed.

RELATED APPLICATIONS

This application is a divisional application of U.S. patent applicationSer. No. 11/055,248, filed Feb. 10, 2005, which in turn claims thebenefit and priority of U.S. provisional application 60/544,579 filedFeb. 13, 2004.

STATEMENT REGARDING FEDERAL RIGHTS

This invention was made with government support under Contract No.W-7405-ENG-36 awarded by the U.S. Department of Energy. The governmenthas certain rights in the invention.

FIELD OF THE INVENTION

The present invention relates generally to primary explosives and moreparticularly to lead-free primary explosives.

BACKGROUND OF THE INVENTION

Primary explosives are substances used in small quantities that whensubjected to a flame, heat, impact, friction or an electric spark,generate a detonation wave. The detonation of the primary explosiveinitiates the secondary or main charge explosive or propellant. The mainrequirements for initiating explosives are sufficient sensitivity to bedetonated reliably but not so sensitive as to be exceedingly dangerousto handle and sufficient thermal stability to not decompose on extendedstorage or thermal insult. Unfortunately, almost all currently usedprimaries contain lead in the form of either lead styphnate or leadazide. Devices using primary explosives are manufactured by the tens ofmillion every year in the U.S. from primers for bullets to detonatorsfor mining. Lead contamination at artillery ranges, both military andcivilian, has become a major environmental issue.

Accordingly, the development of a lead-free primary explosive and aprocess of preparing a lead-free primary explosive have been sought.

SUMMARY OF THE INVENTION

In accordance with the purposes of the present invention, as embodiedand broadly described herein, the present invention includes a compoundof the formula (Cat)⁺ _(z)[M⁺⁺(5-nitro-1H-tetrazolato-N2)⁻_(x)(H₂O)_(y)] where x is 3 or 4, y is 2 or 3, x+y is 6, z is 1 or 2,M⁺⁺ is selected from the group consisting of iron, cobalt, nickel,copper, zinc, chromium, and manganese, and (Cat)⁺ is selected from thegroup consisting of ammonium, sodium, potassium, rubidium and cesium.

The present invention also includes a method of preparing metalcomplexes of the formula (Cat)⁺ _(z)[M⁺⁺(5-nitro-1H-tetrazolato-N2)⁻_(x)(H₂O)_(y)] where x is 3 or 4, y is to 2 or 3, x+y is 6, z is 1 or 2,and M⁺⁺ is selected from the group consisting of iron, cobalt, nickel,copper, zinc, chromium, and manganese, and (Cat)⁺ is selected from thegroup consisting of ammonium, sodium, potassium, rubidium and cesiumincluding admixing a metal salt and a salt of 5-nitrotetrazole in asuitable solvent, and, heating said admixture at temperatures and fortime sufficient to form said metal complexes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows structures of representative species of compounds of thepresent invention.

DETAILED DESCRIPTION

The present invention is concerned with primary explosives and inparticular lead-free primary explosives. Among particular species of thelead-free primary explosives of the present invention are included thecobalt(II), nickel(II), iron(II) and copper(II) complexes shown inFIG. 1. Among particular species are included ammoniumtriaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II), ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II), ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II), ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II), sodiumtriaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II), sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II), sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II), sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II). The complexesinclude a total of six ligands with two or three water ligands and threeor four 5-nitrotetrazolate ligands depending upon the particular centralmetal atom. The compounds of the present invention offer the possibilityof lead-free primary explosives.

The central metals of the compounds of the present invention arenon-toxic. The metals can be selected from among cobalt, nickel, iron,copper, zinc, chromium, and manganese, preferably cobalt, nickel, ironand copper. An iron-based primary explosive has been sought for manyyears and may be most preferable.

The compounds of the present invention can be readily prepared bystirring the particular metal salt in water with the required amount ofa salt of 5-nitrotetrazole, followed by refluxing for a suitable lengthof time, generally about one hour. The resultant complexes precipitateand can be simply filtered and washed with water giving greater than a90 percent yield of analytically pure materials. The composition of thecation, (Cat)⁺, is determined by which salt of 5-nitrotetrazole isutilized. The cation also has an affect on sensitivity and thermalstability with ammonium being the least sensitive and thermally stablewhile the alkali metal salts (sodium, potassium, rubidium and cesium)are more sensitive and thermally stable. All the compounds have thermalstability over 250° C. and densities>2.0 g/cm³. In addition, thesecompounds have no sensitivity to water unlike metastable interstitialcomposite (MIC) based primary explosives. The water in the complexes ischemically bound and does not undergo any further reaction. In fact, thewater may very well be required to “calm down” these materials allowingthem to be worked with safely.

The 5-nitrotetrazolate complex of iron(III) was attempted with nosuccess. It is believed that there is not enough electron density iniron(III) to support a complex ion with the electron deficient ligand of5-nitrotetrazolate.

In the process of the present invention, metal complexes of the formula(Cat)⁺ _(z)[M⁺⁺(5-nitro-1H-tetrazolato-N2)⁻ _(x)(H₂O)_(y)] where x is 3or 4, y is 2 or 3, x+y is 6, z is 1 or 2, and M⁺⁺ is selected from thegroup consisting of iron, cobalt, nickel, copper, zinc, chromium, andmanganese, and (Cat)⁺ is selected from the group consisting of ammonium,sodium, potassium, rubidium and cesium can be prepared by admixing ametal salt and a salt of 5-nitrotetrazole in a suitable solvent, and,heating the admixture at temperatures and for time sufficient to formthe metal complexes. Suitable solvents for the reaction can includewater and may include lower alcohols, with water being the preferredsolvent. The admixture is generally heated at reflux so that with waterit is at about 100° C. and the heating is maintained for about one houralthough the time may be shorter or longer.

Each of the complexes prepared has been compared to the publishedliterature values for lead azide and lead styphnate and the values areshown in Table 1. As can be seen in the Table, each ammonium metalcomplex has a higher detonation velocity than both lead azide and leadstyphnate even though each has lower density. In addition each of theprepared materials is safer to work with than lead azide or leadstyphnate in terms of sensitivity to impact, spark or frictioninitiation, but each is still sensitive enough to be classified as aprimary explosive. The alkali metal salts such as sodium are have alsobeen prepared, and they have comparable thermal stability when comparedto the ammonium is metal salts. Compared to the ammonium metal salts,the sodium metal salts have similar spark sensitivity but are moresensitive to impact and friction. Finally, each of the preparedmaterials, as an ammonium and sodium metal salt, has only slightly lowerthermal stability when compared to lead azide or lead styphnate.However, they are much higher than the minimum temperature requirementof 200° C. Comparative values are given for PETN, which ispentaerythritol tetranitrate.

TABLE 1 Complexes NH₄[Co^(II)(NT)₃(H₂O)₃] (NH₄)₂[Ni^(II)(NT)₄(H₂O)₂](NH₄)₂[Fe^(II)(NT)₄(H₂O)₂] d (g/cm³) 2.04 (Gas Pyc) 2.44 (Gas Pyc) 2.18(Gas Pyc) V_(D) (km/sec) 6.74 (@ 1.64 g/cm³) 7.02 (@ 1.73 g/cm³) 7.14 (@1.71 g/cm³) Spark (J) >0.36 >0.36 >0.36 Friction (kg) 0.8 (vs 5.8 forPETN) 1.5 (vs 5.8 for PETN) 2.8 (vs 5.8 for PETN) Impact (cm) 22 (vs 14for PETN) 18 (vs 14 for PETN) 25 (vs 14 for PETN) DSC 270° C. 270° C.255° C. Complexes NH₄[Cu^(II)(NT)₄(H₂O)₂] [Pb^(II)(N₃)₂][Pb^(II)(styphnate)]•H₂O d (g/cm³) 1.94 (Gas Pyc) 4.80 (X-ray) 3.02(X-ray) V_(D) (km/sec) 7.39 (@ 1.71 g/cm³) 5.5 (@ 3.8 g/cm³) 5.2 (@ 2.9g/cm³) Spark (J) >0.36 0.0047 0.0002 Friction (kg) 0.6 (vs 5.8 for PETN)0.01 (vs 5.8 for PETN) 0.04 (vs 5.8 for PETN) Impact (cm) 22 (vs 14 forPETN) 9.6 (vs 14 for PETN) 14.0 (vs 14 for PETN) DSC 265° C. 315° C.282° C. Complexes Na[Co^(II)(NT)₃(H₂O)₃] Na₂[Ni^(II)(NT)₄(H₂O)₂]Na₂[Fe^(II)(NT)₄(H₂O)₂] Spark (J) >0.36 >0.36 >0.36 Friction (kg) <<0.5<<0.5 <<0.5 Impact (1 oz- Positive Positive Positive 3 in ball-drop) DSC264° C. 265° C. 250° C. Complexes Na₂[Cu^(II)(NT)₄(H₂O)₂] Spark(J) >0.36 Friction (kg) <<0.5 Impact (1 oz- Positive 3 in ball-drop) DSC259° C.

The present invention is more particularly described in the followingexamples, which are intended as illustrative only since numerousmodifications and variations will be apparent to those skilled in theart.

All compounds are sensitive primary explosives and should be worked withonly behind appropriate shielding. All metal salts were obtained fromcommercial sources. Ammonium nitrotetrazolate was prepared bydiazotization of 5-aminotetrazole in the presence of excess nitritefollowed by extraction as the tri-laurylamine salt and displacement byammonia. Upon addition of stoichiometric amount of ammonium hydroxide,sodium nitrotetrazolate forms quantitatively and is analytically pure.Elemental analysis was performed at Los Alamos National Laboratory. Thedata were in agreement to at least two elements within ±0.4%. Meltingpoints were determined by differential scanning calorimetry (DSC) at 5°C./min. Densities were determined by helium gas pycnometry (Gas Pyc).Detonation velocities were determined on 0.25-inch (for cobalt, nickeland copper salts) and 0.5-inch (for iron salt) diameter pellets. Impactsensitivities were determined with a 2.5 kg weight (Type 12, cm) for theammonium metal salts and 1 oz-3 in ball-drop test for the sodium metalsalts. Friction sensitivities were determined with a BAM frictionmachine. Spark sensitivities were determined at 0.36J. The sensitivityand performance values for lead azide and lead styphnate shown in Table1 were taken from the published literature.

Example 1

Preparation of ammoniumtriaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II) as follows. Asolution of 0.501 g (1.72 mmol) hexaaquacobalt(II) perchlorate wasdissolved in 30 ml of water and 0.682 g (5.17 mmol) of ammonium5-nitrotetrazolate added with stirring. A pale yellow precipitate formedimmediately. The suspension was brought to reflux for 2 hrs. Thesolution was cooled to room temperature. The solid was filtered, washedwith water and methanol, and air-dried. Yield 0.74 g (91%). AnalyticallyCalculated for CoC₃H₁₀O₉N₁₆: C, 7.62; H, 2.13; N, 47.37; O, 30.43.Found: C, 7.84; H, 1.82; N, 47.38; O, 29.62.

Example 2

Preparation of ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II) was as follows. Asolution of 0.502 g (1.73 mmol) hexaaquanickel(1I) nitrate was dissolvedin 30 ml of water and 0.912 g (6.90 mmol) of ammonium 5-nitrotetrazolateadded with stirring. A lavender precipitate formed immediately. Thesuspension was brought to reflux for 2 hrs. The solution was cooled toroom temperature. The solid was filtered, washed with water andmethanol, and air-dried. Yield 0.94 g (93%). Analytically Calculated forNiC₄H₁₂O₁₀N₂₂: C, 8.19; H, 2.06; N, 52.50; O, 27.26. Found: C, 7.99; H,1.81; N, 48.22; O, 25.23.

Example 3

Preparation of ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II) was as follows. Asolution of 0.500 g (1.38 mmol) hexaaquairon(II) perchlorate wasdissolved in 30 ml of water and 0.727 g (5.50 mmol) of ammonium5-nitrotetrazolate added with stirring. An orange precipitate formedimmediately. The suspension was brought to reflux for 2 hrs. Thesolution was cooled to room temperature. The solid was filtered, washedwith water and methanol, and air-dried. Yield 0.77 g (96%). AnalyticallyCalculated for FeC₄H₁₂O₁₀N₂₂: C, 8.22; H, 2.07; N, 52.75; O, 27.39.Found: C, 8.29; H, 1.79; N, 48.96; O, 27.62.

Example 4

Preparation of ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II) was as follows. Asolution of 0.500 g (2.07 mmol) hexaaquacopper(II) nitrate was dissolvedin 30 ml of water and 1.09 g (8.28 mmol) of ammonium 5-nitrotetrazolateadded with stirring. A blue precipitate formed immediately. Thesuspension was brought to reflux for 2 hrs. The solution was cooled toroom temperature. The solid was filtered, washed with water andmethanol, and air-dried. Yield 1.14 g (93%). Analytically Calculated forCuC₄H₁₂O₁₀N₂₂: C, 8.12; H, 2.04; N, 52.07; O, 27.03. Found: C, 8.06; H,1.80; N, 48.65; 0, 27.73.

Example 5

Preparation of sodiumtriaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II) was as follows. Asolution of 0.500 g (1.72 mmol) hexaaquacobalt(II) perchlorate wasdissolved in 30 ml of water and 0.892 g (5.15 mmol) of sodium5-nitrotetrazolate added with stirring. A pale yellow precipitate formedimmediately. The suspension was brought to reflux for 2 hrs. Thesolution was cooled to room temperature. The solid was filtered, washedwith water and methanol, and air-dried. Yield 0.76 g (92%).

Example 6

Preparation of sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II) was as follows. Asolution of 0.500 g (1.72 mmol) hexaaquanickel(II) nitrate was dissolvedin 30 ml of water and 1.19 g (6.90 mmol) of sodium 5-nitrotetrazolateadded with stirring. A lavender precipitate formed immediately. Thesuspension was brought to reflux for 2 hrs. The solution was cooled toroom temperature. The solid was filtered, washed with water andmethanol, and air-dried. Yield 0.92 g (90%).

Example 7

Preparation of sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II) was as follows. Asolution of 0.500 g (1.38 mmol) hexaaquairon(II) perchlorate wasdissolved in 30 ml of water and 0.954 g (5.51 mmol) of sodium5-nitrotetrazolate added with stirring. An orange precipitate formedimmediately. The suspension was brought to reflux for 2 hrs. Thesolution was cooled to room temperature. The solid was filtered, washedwith water and methanol, and air-dried. Yield 0.77 g (94%).

Example 8

Preparation of sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II) was as follows. Asolution of 0.500 g (2.07 mmol) hexaaquacopper(II) nitrate was dissolvedin 30 ml of water and 1.43 g (8.28 mmol) of sodium 5-nitrotetrazolateadded with stirring. A blue precipitate formed immediately. Thesuspension was brought to reflux for 2 hrs. The solution was cooled toroom temperature. The solid was filtered, washed with water andmethanol, and air-dried. Yield 1.18 g (95%).

Although the present invention has been described with reference tospecific details, it is not intended that such details should beregarded as limitations upon the scope of the invention, except as andto the extent that they are included in the accompanying claims.

1. A compound of the formula (Cat)⁺ _(z)[M⁺⁺(5-nitro-1H-tetrazolato-N2)⁻_(x)(H₂O)_(y)] where x is 3 or 4, y is 2 or 3, x+y is 6, z is 1 or 2,and M⁺⁺ is selected from the group consisting of iron, cobalt, nickel,copper, zinc, chromium, and manganese, and (Cat)⁺ is selected from thegroup consisting of ammonium, sodium, potassium, rubidium and cesium. 2.The compound, ammoniumtriaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II).
 3. The compound,ammonium diaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II).
 4. Thecompound, ammonium diaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II).5. The compound, ammoniumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II).
 6. The compound,sodium triaquatris(5-nitro-1H-tetrazolato-N2)cobaltate(II).
 7. Thecompound, sodium diaquatetrakis(5-nitro-1H-tetrazolato-N2)nickelate(II).8. The compound, sodiumdiaquatetrakis(5-nitro-1H-tetrazolato-N2)ferrate(II).
 9. The compound,sodium diaquatetrakis(5-nitro-1H-tetrazolato-N2)cuprate(II).